From Optical Activity in Quartz to Chiral Drugs: Molecular Handedness in Biology and Medicine
Buy Issue for $25 at JHUP- From Optical Activity in Quartz to Chiral Drugs:Molecular Handedness in Biology and Medicine
Ronald Bentley, Professor Emeritus
Department of Biological Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania 15260
References
1. BROWNE, M. W. "Mirror image" chemistry yielding new products. The New York Times, 13 Aug. 1991, sect. B: 5, 8.
Google Scholar
2. FDA's policy statement for the development of new stereoisomeric drugs. Chirality 4:338-340, 1992.
Google Scholar
3. FEDER, B. J. Separating "mirror" molecules for better drugs. The New York Times, 12 Feb. 1992, sect. C: 7.
Google Scholar
4. LEWIN, R. Chemistry in the image of biology. Science 238:611-612, 1987.
Google Scholar
5. CHAIKEN, I.; CHIANCONE, E.; FONTANA, A.; and NERI, P., eds. Macromolecular Biorecognition: Principles and Methods. Clifton, N.J.: Humana Press, 1987.
Google Scholar
6. ROBERTS, S. M., ed. Molecular Recognition: Chemical and Biochemical Problems. Vols. I, II. Cambridge: Royal Society of Chemistry, 1989, 1992.
Google Scholar
7. HOLMSTEDT, B.; FRANK, H.; and TESTA, B., eds. Chirality and Biological Activity. New York: A. R. Liss, 1990.
Google Scholar
8. BROWN, C., ed. Chirality in Drug Design and Synthesis. San Diego: Academic Press, 1991.
Google Scholar
9. WILSON, K., and WALKER, J. Chirality and its importance in drug development. Biochem. Soc. Trans. 19:443-474, 1991.
Google Scholar
10. SHELDON, R. A. Chirotechnology: Industrial Synthesis of Optically Active Compounds. New York: M. Dekker, 1993.
Google Scholar
11. AMATO, I. Looking glass chemistry. Science 256:964-966, 1992.
Google Scholar
12. CAHN, R. S.; INGOLD, C.; and PRELOG, V. Specification of molecular chirality. Angew. Chem. Internat. Edit. 5:385-415, 1966.
Google Scholar
13. MISLOW, K. Introduction to Stereochemistry. New York: W. A. Benjamin, 1965.
Google Scholar
14. BIELLMANN, J.-F. Chiralité du diptérocarpol en C-20. Tetrahedron Letters, 4803-4805, 1966.
Google Scholar
15. MACDERMOTT, A. J. Distinguishing true chirality from its accidental imitators. Nature 323:16-17, 1986.
Google Scholar
16. BARRON, L. D. True and false chirality and absolute asymmetric synthesis. J. Amer. Chem. Soc. 108:5539-5542, 1986.
Google Scholar
17. KYBA, E. P.; SIEGEL, M. G.; SOUSA, L. R.; et al. Chiral, hinged, and functionalized multiheteromacrocycles. J. Amer. Chem. Soc. 95:2691-2692, 1973.
Google Scholar
18. KYBA, E. P.; KOGA, K.; SOUSA, L. R.; et al. Chiral recognition in molecular complexing. J. Amer. Chem. Soc. 95:2692-2693, 1973.
Google Scholar
19. JOB, R., and BRUICE, T. C. Chiral recognition of a prochiral (meso-carbon) centre by Λ(—)436-α-l,l-2,9-diamino-4,7-diazadecanecobaltate. J. Chem. Soc. Chem. Comm. 332-333, 1973.
Google Scholar
20. HERSCHEL, J. F. W. On the rotation impressed by plates of rock crystal on the planes of polarization of the rays of light, as connected with certain peculiarities in its crystallization. Trans. Camb. Phil. Soc. 1:43-52, 1822.
Google Scholar
21. PASTEUR, L. Researches on the Molecular Asymmetry of Natural Organic Products. Reissue edition published for the Alembic Club. Edinburgh: E. & S. Livingstone, 1948.
Google Scholar
22. JAPP, F. R. Stereochemistry and vitalism. Nature 58:452-460, 1898.
Google Scholar
23. HANEIN, D.; GEIGER, B.; and ADDADI, L. Differential adhesion of cells to enantiomorphous crystal surfaces. Science 263:1413-1416, 1994.
Google Scholar
24. FRANKLAND, P. Pasteur Memorial Lecture. J. Chem. Soc. Trans. 71:683-743, 1897.
Google Scholar
25. FISCHER, E. Ueber die Spaltung einiger racemischer Amidosäuren in die optisch-activen Componenten. Ber. dtsch. chem. Ges. 32:2451-2471, 1899.
Google Scholar
26. FISCHER, E. Synthesen in der Zuckergruppe. Ber. dtsch. chem. Ges. 23:2114-2141, 1890.
Google Scholar
27. FISCHER, E. Einfluss der Configuration auf die Wirkung der Enzyme. Ber. dtsch. chem. Ges. 27:2985-2993, 1894.
Google Scholar
28. FISCHER, E., and BERGELL, P. Ueber die Derivate einiger Dipeptide und ihr Verhalten gegen Pankreasfermente. Ber. dtsch. chem. Ges. 33:2592-2608, 1903.
Google Scholar
29. DAKIN, H. D. The hydrolysis of optically inactive esters...
